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   The genome of mycobacterium Africanum West African 2 reveals a lineage-specific locus and genome erosion common to the M. tuberculosis complex  
   
نویسنده bentley s.d. ,comas i. ,bryant j.m. ,walker d. ,smith n.h. ,harris s.r. ,thurston s. ,gagneux s. ,wood j. ,antonio m. ,quail m.a. ,gehre f. ,adegbola r.a. ,parkhill j. ,de jong b.c.
منبع plos neglected tropical diseases - 2012 - دوره : 6 - شماره : 2
چکیده    Background: m. africanum west african 2 constitutes an ancient lineage of the m. tuberculosis complex that commonly causes human tuberculosis in west africa and has an attenuated phenotype relative to m. tuberculosis. methodology/principal findings: in search of candidate genes underlying these differences,the genome of m. africanum west african 2 was sequenced using classical capillary sequencing techniques. our findings reveal a unique sequence,rd900,that was independently lost during the evolution of two important lineages within the complex: the modern m. tuberculosis group and the lineage leading to m. bovis. closely related to m. bovis and other animal strains within the m. tuberculosis complex,m. africanum west african 2 shares an abundance of pseudogenes with m. bovis but also with m. africanum west african clade 1. comparison with other strains of the m. tuberculosis complex revealed pseudogenes events in all the known lineages pointing toward ongoing genome erosion likely due to increased genetic drift and relaxed selection linked to serial transmission-bottlenecks and an intracellular lifestyle. conclusions/significance: the genomic differences identified between m. africanum west african 2 and the other strains of the mycobacterium tuberculosis complex may explain its attenuated phenotype,and pave the way for targeted experiments to elucidate the phenotypic characteristic of m. africanum. moreover,availability of the whole genome data allows for verification of conservation of targets used for the next generation of diagnostics and vaccines,in order to ensure similar efficacy in west africa. © 2012 bentley et al.
آدرس wellcome trust genome campus,wellcome trust sanger institute,hinxton, United Kingdom, genomics and health unit,centre for public health research,valencia,spain,division of mycobacterial research,mrc national institute for medical research,the ridgeway,mill hill,london, United Kingdom, wellcome trust genome campus,wellcome trust sanger institute,hinxton, United Kingdom, wellcome trust genome campus,wellcome trust sanger institute,hinxton, United Kingdom, tb research group,veterinary laboratories agency (vla),weybridge,new haw,addlestone,surrey,united kingdom,the centre for the study of evolution,university of sussex,brighton, United Kingdom, wellcome trust genome campus,wellcome trust sanger institute,hinxton, United Kingdom, wellcome trust genome campus,wellcome trust sanger institute,hinxton, United Kingdom, department of medical parasitology and infection biology,swiss tropical and public health institute,basel,switzerland,university of basel,basel, Switzerland, wellcome trust genome campus,wellcome trust sanger institute,hinxton, United Kingdom, vaccinology theme,mrc unit,banjul, Gambia, wellcome trust genome campus,wellcome trust sanger institute,hinxton, United Kingdom, vaccinology theme,mrc unit,banjul,gambia,institute of tropical medicine,antwerp, Belgium, vaccinology theme,mrc unit,banjul, Gambia, wellcome trust genome campus,wellcome trust sanger institute,hinxton, United Kingdom, vaccinology theme,mrc unit,banjul,gambia,institute of tropical medicine,antwerp,belgium,new york university,new york,ny, United States
 
     
   
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